-
1
-
-
0019230239
-
The epidemiology of thyrotoxicosis in Denmark. The incidence and geographical variation in the County of Funen in 1972-1974
-
Mogensen EF, Green A. The epidemiology of thyrotoxicosis in Denmark. The incidence and geographical variation in the County of Funen in 1972-1974. Ugeskrift for Laeger 1980; 142: 1077-80
-
(1980)
Ugeskrift for Laeger
, vol.142
, pp. 1077-1080
-
-
Mogensen, E.F.1
Green, A.2
-
3
-
-
0028228869
-
Incidence of juvenile thyrotoxicoses in Denmark 1982-88
-
Lavard L, Ranløv I, Perrild H, Andersen O, Jacobsen BB. Incidence of juvenile thyrotoxicoses in Denmark 1982-88. Eur J Endocrinol 1994; 130: 565-8
-
(1994)
Eur J Endocrinol
, vol.130
, pp. 565-568
-
-
Lavard, L.1
Ranløv, I.2
Perrild, H.3
Andersen, O.4
Jacobsen, B.B.5
-
4
-
-
0028240982
-
Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism
-
Duprez L, Parma J, van Sande J, Allgeier A, Leclere J, Vassart G, et al. Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism. Nature Genetics 1994; 7: 396-401
-
(1994)
Nature Genetics
, vol.7
, pp. 396-401
-
-
Duprez, L.1
Parma, J.2
Van Sande, J.3
Allgeier, A.4
Leclere, J.5
Vassart, G.6
-
5
-
-
0028891649
-
Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene
-
Kopp P, Van Sande J, Parma J, Duprez L, Gerber H, Vassart G, et al. Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene. N Engl J Med 1995; 332: 150-4
-
(1995)
N Engl J Med
, vol.332
, pp. 150-154
-
-
Kopp, P.1
Van Sande, J.2
Parma, J.3
Duprez, L.4
Gerber, H.5
Vassart, G.6
-
6
-
-
0030715694
-
Sporadic congenital hyperthyroidism due to a spontanous germline mutation in the thyrotropin receptor gene
-
Holzapfel HP, Wonerow P, Petrykowski W, Henschen M, Scherbaum WA, Paschke R. Sporadic congenital hyperthyroidism due to a spontanous germline mutation in the thyrotropin receptor gene. J Clin Endocrinol Metab 1997; 82: 3879-84
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3879-3884
-
-
Holzapfel, H.P.1
Wonerow, P.2
Petrykowski, W.3
Henschen, M.4
Scherbaum, W.A.5
Paschke, R.6
-
7
-
-
0029973239
-
A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism
-
Roux N, Polak M, Couet J, Leger J, Czernichow P, Milgrom E, et al. A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism. J Clin Endocrinol 1996; 81: 2023-6
-
(1996)
J Clin Endocrinol
, vol.81
, pp. 2023-2026
-
-
Roux, N.1
Polak, M.2
Couet, J.3
Leger, J.4
Czernichow, P.5
Milgrom, E.6
-
8
-
-
0032891212
-
Long-term follow-up of an infant with thyrotoxicosis due to germline mutation of the TSH receptor gene (Met453Thr)
-
Lavard L, Sehested A, Brock Jacobsen B, Perrild H, Parma J, Vassart G, et al. Long-term follow-up of an infant with thyrotoxicosis due to germline mutation of the TSH receptor gene (Met453Thr). Horm Res 1998; 51: 43-6
-
(1998)
Horm Res
, vol.51
, pp. 43-46
-
-
Lavard, L.1
Sehested, A.2
Brock Jacobsen, B.3
Perrild, H.4
Parma, J.5
Vassart, G.6
-
9
-
-
8544221172
-
Diversity and prevalence of somatic mutations in the TSH receptor and Gs alpha genes as a cause of toxic thyroid adenomas
-
Parma J, Duprez L, van Sande J, Hermans J, Rocmans P, Vassart G, et al. Diversity and prevalence of somatic mutations in the TSH receptor and Gs alpha genes as a cause of toxic thyroid adenomas. J Clin Endocrinol Metab 1997; 82: 2695-701
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 2695-2701
-
-
Parma, J.1
Duprez, L.2
Van Sande, J.3
Hermans, J.4
Rocmans, P.5
Vassart, G.6
-
10
-
-
0033709508
-
Prevalence of thyroid peroxidase, thyroglobulin and TSH receptor antibodies in a long-term follow-up of juvenile Graves' disease
-
Lavard L, Perrild H, Jacobsen BB, Høier-Madsen M, Bendinelli G, Vitti P. Prevalence of thyroid peroxidase, thyroglobulin and TSH receptor antibodies in a long-term follow-up of juvenile Graves' disease. Autoimmunity 2000; 32: 167-72
-
(2000)
Autoimmunity
, vol.32
, pp. 167-172
-
-
Lavard, L.1
Perrild, H.2
Jacobsen, B.B.3
Høier-Madsen, M.4
Bendinelli, G.5
Vitti, P.6
-
11
-
-
0030710212
-
Somatic mutations in the thyrotropin receptor gene and not in the Gs-alfa protein gene in 31 toxic thyroid nodules
-
Fuhrer D, Holzapfel HP, Wonerow P, Scherbaum WS, Paschke R. Somatic mutations in the thyrotropin receptor gene and not in the Gs-alfa protein gene in 31 toxic thyroid nodules. J Clin Endocrinol Metab 1997; 82: 3885-91
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3885-3891
-
-
Fuhrer, D.1
Holzapfel, H.P.2
Wonerow, P.3
Scherbaum, W.S.4
Paschke, R.5
-
12
-
-
0031014717
-
Two Autonomous nodules of a patient with multinodular goite harbor different activating mutations of the thyrotropin receptor gene
-
Duprez L, Hermans J, van Sande J, Dumont JE, Vassart G, Parma J. Two Autonomous nodules of a patient with multinodular goite harbor different activating mutations of the thyrotropin receptor gene. J Clin Endocrinol Metab 1997; 82: 306-8
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 306-308
-
-
Duprez, L.1
Hermans, J.2
Van Sande, J.3
Dumont, J.E.4
Vassart, G.5
Parma, J.6
-
13
-
-
0030735543
-
Identification of constitutively activating somatic thyrotropin receptor mutations in a subset of toxic multinodular goiters
-
Holzapfel HP, Fuhrer D, Wonerow P, Weinland G, Scherbaum WA, Paschke R. Identification of constitutively activating somatic thyrotropin receptor mutations in a subset of toxic multinodular goiters. J Clin Endocrinol Metab 1997; 82: 4229-33
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 4229-4233
-
-
Holzapfel, H.P.1
Fuhrer, D.2
Wonerow, P.3
Weinland, G.4
Scherbaum, W.A.5
Paschke, R.6
-
14
-
-
2642703472
-
Deletions in the third intracellular loop of the thyrotropin receptor
-
Wonerow P, Schoneberg T, Schultz G, Gudermann T, Paschke R. Deletions in the third intracellular loop of the thyrotropin receptor. J Biol Chem 1998; 273: 7900-5
-
(1998)
J Biol Chem
, vol.273
, pp. 7900-7905
-
-
Wonerow, P.1
Schoneberg, T.2
Schultz, G.3
Gudermann, T.4
Paschke, R.5
-
15
-
-
15144351998
-
Hyperfunctioning thyroid nodules in toxic multinodular goite share activating thyrotropin receptor mutations with solitary toxic adenoma
-
Tonacchera M, Chiovato L, Pinchera A, Agretti P, Fiore E, Cetani F, et al. Hyperfunctioning thyroid nodules in toxic multinodular goite share activating thyrotropin receptor mutations with solitary toxic adenoma. J Clin Endocrinol Metab 1998; 83: 492-8
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 492-498
-
-
Tonacchera, M.1
Chiovato, L.2
Pinchera, A.3
Agretti, P.4
Fiore, E.5
Cetani, F.6
-
16
-
-
13144255717
-
Activating thyrotropin receptor mutations in histologically heterogenous hyperfunctioning nodules of multi-nodular goiter
-
Tonacchera M, Vitti P, Agretti P, Giulianetti B, Mazzi B, Cavaliere R et al. Activating thyrotropin receptor mutations in histologically heterogenous hyperfunctioning nodules of multi-nodular goiter. Thyroid 1998; 8: 559-64
-
(1998)
Thyroid
, vol.8
, pp. 559-564
-
-
Tonacchera, M.1
Vitti, P.2
Agretti, P.3
Giulianetti, B.4
Mazzi, B.5
Cavaliere, R.6
-
17
-
-
0023097627
-
A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA
-
Vassart G, Georges M, Monsieur R, Brocas H, Lequarre AS, Christophe D. A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA. Scisnce 1987; 235: 683-4
-
(1987)
Scisnce
, vol.235
, pp. 683-684
-
-
Vassart, G.1
Georges, M.2
Monsieur, R.3
Brocas, H.4
Lequarre, A.S.5
Christophe, D.6
-
18
-
-
0029874025
-
Micro satellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene
-
Roux N, Misrahi M, Chatelain N, Gross B, Milgrom E. Micro satellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene. Mol Cell Endocrinol 1996; 117: 253-6
-
(1996)
Mol Cell Endocrinol
, vol.117
, pp. 253-256
-
-
Roux, N.1
Misrahi, M.2
Chatelain, N.3
Gross, B.4
Milgrom, E.5
|